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Spontaneous Regression And Resolution Of Breast Implant- Associated Anaplastic Large Cell Lymphoma: Implications For Research, Diagnosis And Clinical Management

Fleming et al., 2018Lymphoma

Fleming, D., Stone, J., & Tansley, P. (2018). spontaneous Regression and Resolution of Breast Implant-Associated Anaplastic Large Cell Lymphoma: Implications for Research, Diagnosis and Clinical Management. Aesthetic plastic surgery, 42(3), 672–678. https://doi.org/10.1007/s00266-017-1064-z

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Abstract

BackgroundFirst described in 1997, breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) was recognised by the World Health Organisation in 2016 as a specific disease. It typically presents as a late seroma-containing atypical, monoclonal T cells which are CD30+ and anaplastic lymphoma kinase negative. Until recently, it was thought that the disease was very rare. However, it is being diagnosed increasingly frequently with 56 cases confirmed in Australia by September 2017 and the estimated incidence revised from 1 in 300,000 to between 1 in 1000 and 1 in 10,000 patients with bilateral implants. There is debate about the spectrum of BIA-ALCL. According to the current WHO classification, BIA-ALCL is a cancer in all cases. Treatment guidelines require that it is treated urgently with a minimum of bilateral removal of implants and capsulectomies. Whilst acknowledging the disease has been under diagnosed in the past, with some notable exceptions the BIA-ALCL literature has given scant attention to the epidemiological evidence. Now that it is known that the disease may occur in up to 1 in 1000 patients with a median of 7.5 years from implantation to diagnosis, understanding it in its epidemiological context is imperative. The epidemiology of cancer and lymphoma in women with breast implants strongly suggests that most patients do not have a cancer that will inevitably progress without treatment but instead a self-limiting lympho-proliferative disorder. Although the possibility of spontaneous regression has been raised and the observation made that treatment delay did not seem to increase the risk of spread, the main objection to the lympho-proliferative hypothesis has been the lack of documented cases of spontaneous regression or resolution. Because all cases currently are considered malignant and treated urgently, only case report evidence, interpreted in the proper epidemiological context, is likely to be available to challenge this thinking.Methods and ResultsNew observations and interpretation of the epidemiology of BIA-ALCL are made. These are supported by the presentation of two cases, which to the best of our knowledge comprise the first documented evidence of spontaneous regression and spontaneous resolution of confirmed BIA-ALCL.ConclusionsThe epidemiology of the disease strongly suggests that the vast majority of cases are not a cancer that will inevitably progress without treatment. The findings presented in the manuscript provide supportive clinical evidence. Consequently, an alternative view of BIA-ALCL with implications for research, diagnosis and clinical management needs to be considered.Level of Evidence IVThis journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.

Case Details

Disease Location

Right breast

Personal Characteristics

51 -year-old female in 1994 (age 32), she underwent bilateral, subglandular breast augmentation and concomitant periareolar mastopexy using mentor, smooth, saline implants. A left sided post-op wound infection was treated conservatively, she developed bilateral capsular contracture after some months in 2009, she underwent bilateral explantation and replacement with silimed, polyurethane foam-covered silicone gel implants in new submuscular pockets. The left capsule was heavily calcified and excised, the right capsule was retained.

Clinical Characteristics

Breast implant-assoicated anaplastic large cell lymphoma (bia-alcl) in may 2014 (age 51) she presented with a unilateral enlargement of the right breast an ultrasound demonstrated the presence of a large seroma she delayed seeking treatment for 8 months until january 2015 when she underwent aspiration cytology was diagnostic for bia-alcl with abundant atypical t cells that were CD30+ 2 months later in march 2015, aspiration was repeated. Most cells identified were benign macrophages. The very scant CD30+ cells identified were interpreted as representing a combination of benign activated lymphocytes and a very ow level of lymphoma <5% in april 2015 she underwent breast implant explanation and capsulectomy at surgery, occasional atypical lymphoid cells were identified on cytological exam of the greatly reduced residual seroma fluid. The fluid was paucicellular and there was insufficient cellular material for reliable ihc exam

Remission Characteristics

Since surgery in 2015, she has remained asymptomatic

Treatment & Mechanisms

Proposed Remission Mechanisms

No major mechanism proposed

Clinical Treatment

Breast implant explanation and capsulectomy

Non-Clinical Treatment

None reported